Evidence map›Paper›PMID 37838079›Full record

ArticleBrain, behavior, and immunity2024

The role of the Toll like receptor 4 signaling in sex-specific persistency of depression-like behavior in response to chronic stress.

Eun-Jeong Yang, Tal Frolinger, Umar Iqbal, Molly Estill, Li Shen, Kyle J Trageser, Giulio M Pasinetti

Open access · hybridAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Eun-Jeong YangDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
Tal FrolingerDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
Umar IqbalDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
Molly EstillDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
Li ShenDepartment of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
Kyle J TrageserDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
Giulio M PasinettiDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States; Geriatric Research, Education and Clinical Center, James J. Peters Veterans Affairs Medical Center, Bronx, New York 10468, United States. Electronic address: giulio.pasinetti@mssm.edu.
Icahn School of Medicine at Mount Sinai · USGeriatric Research Education and Clinical Center · US

Funding

Suppression of Immune Signatures of Stress by Polyphenols SupplementsU19AT010835 · NCCIH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI RUSSO, SCOTT JAMES · 2020 to 2024
$6.8M
Validation of Immune Dysfunction in Model of Social Stress: Implications for Major Depression Disorder in VeteransI01BX005054 · VA · JAMES J PETERS VA MEDICAL CENTER · PI Giulio Maria Pasinetti · 2021 to 2026
–
BLRD VA I01 BX005054NCCIH NIH HHS U19 AT010835
6 · The paper itself

Abstract

Chronic stress is a major risk factor for Major Depressive Disorder (MDD), and it has been shown to impact the immune system and cause microglia activation in the medial prefrontal cortex (mPFC) involved in the pathogenesis of depression. The aim of this study is to further investigate cellular and molecular mechanisms underlying persistent depression behavior in sex specific manner, which is observed clinically. Here, we report that both male and female mice exhibited depression-like behavior following exposure to chronic stress. However, only female mice showed persistent depression-like behavior, which was associated with microglia activation in mPFC, characterized by distinctive alterations in the phenotype of microglia. Given these findings, to further investigate the underlying molecular mechanisms associated with persistent depression-like behavior and microglia activation in female mice, we used translating-ribosome affinity purification (TRAP). We find that Toll like receptor 4 (TLR4) signaling is casually related to persistent depression-like behavior in female mice. This is supported by the evidence that the fact that genetic ablation of TLR4 expression in microglia significantly reduced the persistent depression-like behavior to baseline levels in female mice. This study tentatively supports the hypothesis that the TLR4 signaling in microglia may be responsible for the sex differences in persistent depression-like behavior in female.

Indexed as

DepressionMajor Depressive DisorderToll-Like Receptor 4AnimalsFemaleMaleMiceMicrogliaSignal TransductionStress, PsychologicalToll-Like Receptor 4Chronic stressDepressionMicroglia activationNeuroinflammationSex differenceTLR4

Identifiers

PMID37838079
PMCPMC11146676
OpenAlexW4387580162

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.